Wertz E M, Benson G J, Thurmon J C, Tranquilli W J, Davis L E, Koritz G D
Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois, Urbana 61801.
Am J Vet Res. 1990 Feb;51(2):281-5.
Pharmacokinetic variables of etomidate were determined after IV administration of etomidate (3.0 mg/kg of body weight). Blood samples were collected for 6 hours. Disposition of this carboxylated imidazole best conformed to a 2- (n = 2) and a 3- compartment (n = 4) open pharmacokinetic model. The pharmacokinetic values were calculated for the overall best-fitted model, characterized as a mixed 2- and 3-compartmental model. The first and most rapid distribution half-life was 0.05 hour and a second distribution half-life was 0.35 hour. Elimination half-life was 2.89 hours, apparent volume of distribution was 11.87 +/- 4.64 L/kg, apparent volume of distribution at steady state was 4.88 +/- 2.25 L/kg, apparent volume of the central compartment was 1.17 +/- 0.70 L/kg, and total clearance was 2.47 +/- 0.78 L/kg/h.
在静脉注射依托咪酯(3.0毫克/千克体重)后测定依托咪酯的药代动力学变量。采集血样6小时。这种羧化咪唑的处置最符合二室开放药代动力学模型(n = 2)和三室开放药代动力学模型(n = 4)。为总体最佳拟合模型计算药代动力学值,其特征为混合二室和三室模型。第一个也是最快的分布半衰期为0.05小时,第二个分布半衰期为0.35小时。消除半衰期为2.89小时,表观分布容积为11.87±4.64升/千克,稳态时的表观分布容积为4.88±2.25升/千克,中央室的表观容积为1.17±0.70升/千克,总清除率为2.47±0.78升/千克/小时。